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Medium-throughput image-based phenotypic siRNA screen to unveil the molecular basis of B cell polarization
Indexado
WoS WOS:001013266000003
Scopus SCOPUS_ID:85162830540
DOI 10.1038/S41597-023-02301-0
Año 2023
Tipo artículo de investigación

Citas Totales

Autores Afiliación Chile

Instituciones Chile

% Participación
Internacional

Autores
Afiliación Extranjera

Instituciones
Extranjeras


Abstract



Cell polarity is an essential and highly conserved process governing cell function. Cell polarization is generally triggered by an external signal that induces the relocation of the centrosome, thus defining the polarity axis of the cell. Here, we took advantage of B cells as a model to study cell polarity and perform a medium-throughput siRNA-based imaging screen to identify new molecular regulators of polarization. We first identified candidates based on a quantitative proteomic analysis of proteins differentially associated with the centrosome of resting non-polarized and stimulated polarized B cells. We then targeted 233 candidates in a siRNA screen and identified hits regulating the polarization of the centrosome and/or lysosomes in B cells upon stimulation. Our dataset of proteomics, images, and polarity indexes provides a valuable source of information for a broad community of scientists interested in the molecular mechanisms regulating cell polarity.

Revista



Revista ISSN
Scientific Data 2052-4463

Métricas Externas



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Disciplinas de Investigación



WOS
Multidisciplinary Sciences
Scopus
Sin Disciplinas
SciELO
Sin Disciplinas

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Publicaciones WoS (Ediciones: ISSHP, ISTP, AHCI, SSCI, SCI), Scopus, SciELO Chile.

Colaboración Institucional



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Autores - Afiliación



Ord. Autor Género Institución - País
1 Obino, Dorian Hombre PSL Res Univ - Francia
Immunite et Cancer - Francia
Institut Curie - Francia
2 Maurin, Mathieu Hombre PSL Res Univ - Francia
Immunite et Cancer - Francia
Institut Curie - Francia
3 Dingli, Florent Hombre PSL Res Univ - Francia
Institut Curie - Francia
4 Loew, Damarys - PSL Res Univ - Francia
Institut Curie - Francia
5 Lescure, Aurianne Mujer PSL Res Univ - Francia
Institut Curie - Francia
6 Terriac, Emmanuel Hombre PSL Res Univ - Francia
Biologie Cellulaire et Cancer - Francia
Institut Curie - Francia
7 Goudot, Christel Mujer PSL Res Univ - Francia
Immunite et Cancer - Francia
Institut Curie - Francia
8 Malbec, Odile Mujer PSL Res Univ - Francia
Immunite et Cancer - Francia
Institut Curie - Francia
9 Lankar, Danielle Mujer PSL Res Univ - Francia
Immunite et Cancer - Francia
Institut Curie - Francia
10 Yuseff, Maria-Isabel Mujer PSL Res Univ - Francia
Pontificia Universidad Católica de Chile - Chile
Immunite et Cancer - Francia
Institut Curie - Francia
11 Lennon-Dumenil, Ana-Maria Mujer PSL Res Univ - Francia
Immunite et Cancer - Francia
Institut Curie - Francia
12 Moreau, Helene D. Mujer PSL Res Univ - Francia
Immunite et Cancer - Francia
Institut Curie - Francia

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Financiamiento



Fuente
Institut Pasteur
Institut Curie
Institut National de la Santé et de la Recherche Médicale
Université Paris Diderot
Ecole Doctorale BioSPC
Universite Paris Descartes
INSERM positions
Université Paris Diderot and Université Paris Descartes
Adrian Isaacs (UK Dementia Research Institute at University College London
ANR-PoLyBex-12-BVS3-0014-001
CurieCoreTech Mass Spectrometry Proteomics

Muestra la fuente de financiamiento declarada en la publicación.

Agradecimientos



Agradecimiento
The authors thank Adrian Isaacs (UK Dementia Research Institute at University College London) for kindly providing the Chmp2b-/- mice, Emeline Perthame (Bioinformatics and Biostatistics HUB at Institut Pasteur) for having performed the permutation test, and Michael Richard (CurieCoreTech Mass Spectrometry Proteomics at Institut Curie) and Patrick Poullet (INSERM U900, Institut Curie) for having performed the analysis using the R package SuperExactTest. We acknowledge the members of the Lennon-Dumenil team and Elaine Del Nery for fruitful discussions. The experimental work was funded by ANR-PoLyBex-12-BVS3-0014-001 to AMLD. DO was supported by a fellowship from the Ecole Doctorale BioSPC, Universite Paris Diderot and Universite Paris Descartes. DO and HDM are supported by INSERM positions.
The authors thank Adrian Isaacs (UK Dementia Research Institute at University College London) for kindly providing the Chmp2b−/−mice, Emeline Perthame (Bioinformatics and Biostatistics HUB at Institut Pasteur) for having performed the permutation test, and Michael Richard (CurieCoreTech Mass Spectrometry Proteomics at Institut Curie) and Patrick Poullet (INSERM U900, Institut Curie) for having performed the analysis using the R package SuperExactTest. We acknowledge the members of the Lennon-Duménil team and Elaine Del Nery for fruitful discussions. The experimental work was funded by ANR-PoLyBex-12-BVS3-0014-001 to AMLD. DO was supported by a fellowship from the Ecole Doctorale BioSPC, Université Paris Diderot and Université Paris Descartes. DO and HDM are supported by INSERM positions.
The authors thank Adrian Isaacs (UK Dementia Research Institute at University College London) for kindly providing the Chmp2b−/−mice, Emeline Perthame (Bioinformatics and Biostatistics HUB at Institut Pasteur) for having performed the permutation test, and Michael Richard (CurieCoreTech Mass Spectrometry Proteomics at Institut Curie) and Patrick Poullet (INSERM U900, Institut Curie) for having performed the analysis using the R package SuperExactTest. We acknowledge the members of the Lennon-Duménil team and Elaine Del Nery for fruitful discussions. The experimental work was funded by ANR-PoLyBex-12-BVS3-0014-001 to AMLD. DO was supported by a fellowship from the Ecole Doctorale BioSPC, Université Paris Diderot and Université Paris Descartes. DO and HDM are supported by INSERM positions.

Muestra la fuente de financiamiento declarada en la publicación.